Genomic variant #0000335961

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152086664G>A
DNA change (hg38) -
Published as ZNF185:NM_001178106.1:c.397G>A, NM_001178107.1:c.397G>A, …
ISCN -
DB-ID ZNF185_000052
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Leiden




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
ZNF185 NM_001178106.1 ./. - c.397G>A - r.(?) p.(Gly133Ser)